Recall of A.L.P.S. 4.0mm Cancellous Locking Screws (non-sterile)CNCLS LOCK SCREW FT4.0x10mm, 4.0x12mm, 4.0x14mm, 4.0x16mm, 4.0x18mm, 4.0x20mm, 4.0x22mm ,4.0x24mm, 4.0x26mm, 4.0x28mm, 4.0x30mm, 4.0x32mm, 4.0x34mm, 4.0x36mm, 4.0x38mm, 4.0x40mm, 4.0x42mm, 4.0x44mm, 4.0x46mm, 4.0x48mm, 4.0x50mm, 4.0x55mm, 4.0x60mm, 4.0x65mm, 4.0x70mm, 4.0x75mm, 4.0x80mm, 4.0x85mm, 4.0x90mm, 4.0x95mm, 4.0x100mm

According to Department of Health, Therapeutic Goods Administration, this recall involved a device in Australia that was produced by Biomet Australia Pty Ltd.

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    RC-2015-RN-01162-1
  • Event Risk Class
    Class II
  • Event Initiated Date
    2015-11-30
  • Event Country
  • Event Source
    DHTGA
  • Event Source URL
  • Notes / Alerts
    Australian data is current through July 2018. All of the data comes from the Australian Therapeutic Goods Administration, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Australia.
  • Extra notes in the data
  • Reason
    It has been identified that all lots of a.L.P.S. 4.0mm cancellous locking screws, manufactured between june 1, 2008 and june 4, 2015, have a single lead thread instead of a triple lead thread. a single lead screw may sit proud in the plate which could lead to soft tissue irritation. in addition, if the screw does not lock into the plate, it is possible for the screw to back out. in the event that the screw does not lock into the plate and backs out, a revision surgery may be necessary.
  • Action
    Zimmer Biomet is advising users to inspect stock and quarantine the affected unused units prior to their return to the sponsor. The sponsor will replace the affected unused units. Patients who have been implanted with the affected units should be monitored by qualified healthcare professional. For more details, please see https://www.tga.gov.au/alert/anatomic-locked-plating-system-4-mm-cancellous-locking-screws-used-treat-broken-bones . This action has been closed-out on 29/08/2016.

Device

  • Model / Serial
    A.L.P.S. 4.0mm Cancellous Locking Screws (non-sterile)CNCLS LOCK SCREW FT4.0x10mm, 4.0x12mm, 4.0x14mm, 4.0x16mm, 4.0x18mm, 4.0x20mm, 4.0x22mm ,4.0x24mm, 4.0x26mm, 4.0x28mm, 4.0x30mm, 4.0x32mm, 4.0x34mm, 4.0x36mm, 4.0x38mm, 4.0x40mm, 4.0x42mm, 4.0x44mm, 4.0x46mm, 4.0x48mm, 4.0x50mm, 4.0x55mm, 4.0x60mm, 4.0x65mm, 4.0x70mm, 4.0x75mm, 4.0x80mm, 4.0x85mm, 4.0x90mm, 4.0x95mm, 4.0x100mmMultiple Part Numbers AffectedAll Lot Numbers AffectedARTG Number: 209305
  • Manufacturer

Manufacturer

  • Manufacturer Parent Company (2017)
  • Manufacturer comment
    “The safety of patients has always been, and continues to be, Zimmer Biomet’s top priority and it is our honor to be a leader in this industry for the past 90 years,” Zimmer Biomet told ICIJ in a statement. “We adhere to strict regulatory standards, and work closely with the FDA and all applicable regulatory agencies in each of our regions as part of our commitment to operating a first-rate quality management system across our global manufacturing network. The company added that it is focused on staying at the forefront of innovation and doing right by the millions of patients who rely on the company’s products.
  • Source
    DHTGA